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Regulatory Remediation Associate

£Negotiable DoE | Yorkshire & The Humber |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:888079

The Role

Regulatory Remediation Associate, Global Health &Hygiene Company, Yorkshire, £Negotiable DoE

 

The Company

This is an exciting time to join an expanding, highly successful global healthcare company based at their Yorkshire site. Fantastic refurbished offices with many facilities including staff shop, canteen, subsidised coffee shop and dry cleaners.

  • Excellent career progression opportunities
  • City location with plenty of free onsite parking and close to major transport links
  • Great benefits with bonus, pension, healthcare, share scheme and discounted products.

 

The Role

As the Regulatory Remediation Associate, you will be responsible for;

  • Providing product reviews to ensure compliance with local legislation across a range of products
  • Managing regulatory changes across the product portfolio and managing risks and threats
  • Manage and update stakeholders regularly on the regulatory status of all products.

 

You

As a Regulatory Remediation Associate, you will have the following experience:

  • Good background / knowledge of Regulatory Affairs either within, Pharma or Medical Devices, cosmetics or chemicals
  • Good experience within registration and maintenance of technical documents
  • Post marketing compliance experience
  • Strong stakeholder management be able to liaise with various teams within the business and good influencing skills

 

What should you do next?

This Regulatory Remediation Associate job is a great role and won't be around for long! So don't delay. If you are unsure and need some advice, give me a ring, otherwise just click apply, upload your CV and send, it's really that easy!

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there. Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

Consultant

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Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.

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